Renal hypodysplasia/aplasia 2

MONDO:0014319

Any renal agenesis in which the cause of the disease is a mutation in the FGF20 gene.

Also known as: FGF20 renal agenesis (disease), renal agenesis (disease) caused by mutation in FGF20, renal hypodysplasia/aplasia 2, renal hypodysplasia/aplasia type 2, RHDA2

1 clinical trial for this condition and its sub-types, 0 tagged with Renal hypodysplasia/aplasia 2 itself.

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↑ Renal agenesis (2)

Including sub-types (1) Tagged with Renal hypodysplasia/aplasia 2 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.